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[6R-(6α,7β)]-3-[[[[5-(4-fluorophenyl)-5,8-dihydro-8-oxo-1,3-dioxolo[4,5-g]quinolin-7-yl]carbonyl]oxy]methyl]-8-oxo-7-[(phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115699-51-9

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115699-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115699-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,9 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115699-51:
(8*1)+(7*1)+(6*5)+(5*6)+(4*9)+(3*9)+(2*5)+(1*1)=149
149 % 10 = 9
So 115699-51-9 is a valid CAS Registry Number.

115699-51-9Downstream Products

115699-51-9Relevant academic research and scientific papers

Anti-bacterial cephalosporin compounds

-

, (2008/06/13)

There are presented anti-bacterial cephalosporins having broad antimicrobial activity of the formula STR1 wherein R1 is an antibiotically active quinolonyl; R2 is selected from the group consisting of hydrogen, lower alkoxy, amino, l

Cephalosporin 3'-Quinolone Esters with a Dual Mode of Action

Albrecht, Harry A.,Beskid, George,Chan, Ka-Kong,Christenson, James G.,Cleeland, Roy,et al.

, p. 77 - 86 (2007/10/02)

According to the generally accepted mechanism by which bacterial enzymes react with cephalosporins, opening of the β-lactam ring can lead to the expulsion of a 3'-substituent.A series of dual-action cephalosporins was prepared in which antibacterial quino

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